Clinical Research Physician at Translational Research in Oncology TRIO

Boston, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Jun, 26

Salary

150000.0

Posted On

21 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Monitoring, Oncology, Translational Research, Clinical Trials, Patient Safety, Serious Adverse Events Review, Protocol Deviations Review, Medical Inquiries Response, Scientific Presentation, ICH GCP Guidelines, MS Office Proficiency, Teamwork, Communication Skills, English Proficiency

Industry

Research Services

Description

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in the USA. Main Responsibilities: Act as Medical Monitor, performing comprehensive medical monitoring activities. Respond to medical inquiries from investigational sites and trial teams. Review patient eligibility and protocol deviations. Oversee patient safety by reviewing medical data at patient and trial levels. Review Serious Adverse Events (SAEs), including coding, causality and expectedness assessments, and drafting company comments. Prepares scientific slides, attends and/or presents protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, SIVs, etc. Serve as the primary clinical point of contact for scientific questions from internal and external stakeholders (e.g., IRBs, sites, sponsor medical teams, trial teams). Collaborates with the Medical Writing and Training Unit to write and/or review trial-specific medical documents (e.g., protocols, DSURs, CSRs). Conducting medical training on selected trial-specific or non-trial-specific topics. Qualifications: Medical Doctor degree required Excellent knowledge and understanding of oncology and oncology clinical trials At least 1 year of experience in medical monitoring in oncology trials Current knowledge of ICH GCP guidelines Advanced proficiency in MS Office in Word, Excel, and PowerPoint Strong teamwork abilities and communication skills Excellent level of English is required Spanish language knowledge will be valued Must be legally authorized to work in the country What TRIO Can Offer You: Competitive Salary 3 weeks of vacation plus paid Christmas Closure 2 weeks paid personal/sick time 100% health benefits for you and your family paid by TRIO Flexible working hours Monthly internet allowance 401K Program 5% Salary Contribution Home office allowance Pay Range: $110,000 - $150,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. Prior to applying please review TRIO's Applicant Information Notice To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI. To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience. Teamwork · Passion · Integrity · Innovation

Responsibilities

The Clinical Research Physician will act as the Medical Monitor, performing comprehensive medical monitoring activities such as reviewing patient eligibility, protocol deviations, and overseeing patient safety by reviewing medical data. This role also involves responding to medical inquiries, reviewing Serious Adverse Events, and preparing scientific presentations for various meetings.